A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523680



Internal ID299906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12053727..12066782hg38UCSC Ensembl
chr19:12164542..12177597hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3813056
hg1913056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721469
Samples
Known GenesZNF844
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523680
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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